Meetings/Workshops on Regulation in Medicine and Pharmacology in India

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1.
 
2 Day In-Person Seminar on Computer Systems Validations, Data Integrity, 21 CFR Part 11 Compliance and GAMP 5
ID
875428
Dates
18 Apr 2017 - 19 Apr 2017
Location
Hyderabad, India
Abstract
This new 2-day Seminar on Computer Systems Validation provides participants with knowledge and tools to effectively use, monitor, control, and assure the integrity of electronic data and computerized systems. The presenter - Mr. KR Vaghela will help you explore proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. The course not only ensures a full understanding of the regulations and guidelines for raw data and other records but also provides templates and examples to develop inspection ready documentation. Interactive exercises will be dispersed into and between the presentations.
Contact
Compliance Trainings;     Phone: [8041700521];     Email: info@compliancetrainings.in
Topics
Seminar, Computer Systems Validations, Data Integrity, 21 CFR Part 11 Compliance, FDA GAMP 5, GxP and Part 11 inspections, Annex 11 regulation, 21 CFR Part 11 compliance
2.
 
2nd Annual CAPA & Root Cause Investigation Workshop 201
ID
894151
Dates
20 Apr 2017 - 21 Apr 2017
Location
Mumbai, India
Abstract
Recent warning letters from the FDA states that ineffective CAPA actions are a major reason for non-compliance. Investigating the cause of the quality failure and linking it to the right CAPA will avoid recurrence of discrepancies. Considering the criticality of the situation, we at CPhI bring you the 2nd Annual CAPA & Root Cause Investigation Workshop scheduled on April 20th-21st 2017 in Mumbai with the focus being having a thorough CAPA investigation and thus ensuring a successful audit.
Contact
Sean Palanna;     Phone: [91 22 6172 7072];     Email: sean.palanna@ubm.com
Topics
Deviation Management, CAPA – Effectiveness, periodic verification
Related subject(s)
3.
 
6th Annual Global Pharma Regulatory Summit 2017
ID
894248
Dates
26 Apr 2017 - 28 Apr 2017
Location
Mumbai, India
Abstract
Indian generic drugs market has posted an impressive growth pattern over the last few years. Currently, the Indian pharmaceutical market is fully dominated by generic drugs and in the near future, this scenario is likely to remain the same. The Indian pharmaceuticals market increased at a CAGR of 17.46 per cent during 2005-16 with the market increasing from US$ 6 billion in 2005 to US$ 36.7 billion in 2016 and is expected to expand at a CAGR of 15.92 per cent to US$ 55 billion by 2020. But at the same time there are immense of regulatory concerns raised by the global authorities over the the quality of drugs manufactured in India. Keeping this in mind CPhI India brings you the 6th Edition of Global Pharma Regulatory Summit 2017 scheduled on 26-27-28 April in Mumbai, focusing on the clarification and interpretation to the most critical regulatory guidelines faced by the Indian Pharma companies. This three day strategic summit provides insights on the US, Europe and ROW region which are constitute to the major revenue of the top Indian pharmaceutical companies
Contact
Sean Palanna;     Phone: [91 22 61727072];     Email: sean.palanna@ubm.com
Topics
Pharma regulatory

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Last updated: 23 March 2017